Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_assertion description "[Polymorphisms in NQO1, IL-10 and PTPN11, in combination with HP status, could be used to identify individuals who are more likely to develop IM and therefore GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_assertion evidence source_evidence_literature NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_assertion SIO_000772 19822020 NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_assertion wasDerivedFrom befree-2016 NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_assertion wasGeneratedBy ECO_0000203 NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP768879.RAilwxe0LJSIHjV1HOed26AuISPMFpN2kBrZHzZSDcPsU130_provenance.